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B A Bharucha

Showing results (31-40 of 85) with videos related to

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Indian Pediatrics|May 1, 1983
Siblings with Larsen's syndromeB A Bharucha, A S Savliwala, G V Koppikar, et al.
Journal of Postgraduate Medicine|October 1, 1992
Wildervanck syndrome (cervico-oculo-acoustic syndrome)G Gupte, P Mahajan, V K Shreenivas, et al.
Indian Pediatrics|September 1, 1990
Efficacy of three doses of oral polio immunization beginning within the first four days of lifeA M Bhatawdekar, N B Kumta, K H Dave, et al.
American Journal of Medical Genetics. Part A|February 25, 2003
Ring chromosome 12 with variable phenotypic features: clinical report and review of the literatureRamesh C Parmar, Mamta N Muranjan, S Kotvaliwale, et al.
Indian Journal of Pediatrics|May 8, 2000
Familial glucocorticoid deficiency, alacrimia and achalasia--Allgrove syndromeM N Muranjan, M Gurav, T Surve, et al.
Indian Journal of Pediatrics|July 1, 1994
Storage disorders presenting like mucopolysaccharidosisM U Sanklecha, A Kher, G G Naik, et al.
Clinical Dysmorphology|July 1, 1996
Craniosynostosis with Marfan syndrome, hand and foot anomaliesA M Shah, A Chattopadhyay, A Kher, et al.
Pediatric Cardiology|November 1, 1996
Familial congenital valvar pulmonary stenosis: autosomal dominant inheritanceA D Udwadia, S Khambadkone, B A Bharucha, et al.
Journal of Postgraduate Medicine|July 1, 1992
MURCS association--a review of 7 casesP Mahajan, A Kher, A Khungar, et al.
Indian Journal of Pediatrics|September 1, 1995
Mucolipidoses--II: A report of three casesS G Lalwani, A Kher, N Shridhar, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
Indian Pediatrics|May 1, 1983
Siblings with Larsen's syndromeB A Bharucha, A S Savliwala, G V Koppikar, et al.
Journal of Postgraduate Medicine|October 1, 1992
Wildervanck syndrome (cervico-oculo-acoustic syndrome)G Gupte, P Mahajan, V K Shreenivas, et al.
Indian Pediatrics|September 1, 1990
Efficacy of three doses of oral polio immunization beginning within the first four days of lifeA M Bhatawdekar, N B Kumta, K H Dave, et al.
American Journal of Medical Genetics. Part A|February 25, 2003
Ring chromosome 12 with variable phenotypic features: clinical report and review of the literatureRamesh C Parmar, Mamta N Muranjan, S Kotvaliwale, et al.
Indian Journal of Pediatrics|May 8, 2000
Familial glucocorticoid deficiency, alacrimia and achalasia--Allgrove syndromeM N Muranjan, M Gurav, T Surve, et al.
Indian Journal of Pediatrics|July 1, 1994
Storage disorders presenting like mucopolysaccharidosisM U Sanklecha, A Kher, G G Naik, et al.
Clinical Dysmorphology|July 1, 1996
Craniosynostosis with Marfan syndrome, hand and foot anomaliesA M Shah, A Chattopadhyay, A Kher, et al.
Pediatric Cardiology|November 1, 1996
Familial congenital valvar pulmonary stenosis: autosomal dominant inheritanceA D Udwadia, S Khambadkone, B A Bharucha, et al.
Journal of Postgraduate Medicine|July 1, 1992
MURCS association--a review of 7 casesP Mahajan, A Kher, A Khungar, et al.
Indian Journal of Pediatrics|September 1, 1995
Mucolipidoses--II: A report of three casesS G Lalwani, A Kher, N Shridhar, et al.
Pageof 9